clinical chromosomal microarray database Search Results


chromosomal microarrays (cmas) v8  (Medical Genetics Laboratories)
90
Medical Genetics Laboratories chromosomal microarrays (cmas) v8
Chromosomal Microarrays (Cmas) V8, supplied by Medical Genetics Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/chromosomal microarrays (cmas) v8/product/Medical Genetics Laboratories
Average 90 stars, based on 1 article reviews
chromosomal microarrays (cmas) v8 - by Bioz Stars, 2026-04
90/100 stars
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clinical chromosomal microarray  (Sema4 Inc)
90
Sema4 Inc clinical chromosomal microarray
Illustration of the chromosome 10q23.33 region with the identified CYP2C copy number variants (CNVs) noted in relation to the location of known human genes and transcripts from the UCSC Genes track, segmental duplications, <t>microarray</t> (purple), MLPA (light green), and ddPCR (dark green) probe locations, structural variants from the Database of Genomic Variants (DGV), ClinGen, and DECIPHER. Blue bars represent copy number gains (duplications), red bars represent copy number losses (deletions). The minimum and maximum CNV sizes in the clinical CMA cohorts are denoted by thick and thin horizontal bars, respectively.
Clinical Chromosomal Microarray, supplied by Sema4 Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/clinical chromosomal microarray/product/Sema4 Inc
Average 90 stars, based on 1 article reviews
clinical chromosomal microarray - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
clinical chromosome microarray analysis  (Baylor Genetics)
90
Baylor Genetics clinical chromosome microarray analysis
Illustration of the chromosome 10q23.33 region with the identified CYP2C copy number variants (CNVs) noted in relation to the location of known human genes and transcripts from the UCSC Genes track, segmental duplications, <t>microarray</t> (purple), MLPA (light green), and ddPCR (dark green) probe locations, structural variants from the Database of Genomic Variants (DGV), ClinGen, and DECIPHER. Blue bars represent copy number gains (duplications), red bars represent copy number losses (deletions). The minimum and maximum CNV sizes in the clinical CMA cohorts are denoted by thick and thin horizontal bars, respectively.
Clinical Chromosome Microarray Analysis, supplied by Baylor Genetics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/clinical chromosome microarray analysis/product/Baylor Genetics
Average 90 stars, based on 1 article reviews
clinical chromosome microarray analysis - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

Image Search Results


Illustration of the chromosome 10q23.33 region with the identified CYP2C copy number variants (CNVs) noted in relation to the location of known human genes and transcripts from the UCSC Genes track, segmental duplications, microarray (purple), MLPA (light green), and ddPCR (dark green) probe locations, structural variants from the Database of Genomic Variants (DGV), ClinGen, and DECIPHER. Blue bars represent copy number gains (duplications), red bars represent copy number losses (deletions). The minimum and maximum CNV sizes in the clinical CMA cohorts are denoted by thick and thin horizontal bars, respectively.

Journal: Human mutation

Article Title: Structural variation at the CYP2C locus: Characterization of deletion and duplication alleles

doi: 10.1002/humu.23855

Figure Lengend Snippet: Illustration of the chromosome 10q23.33 region with the identified CYP2C copy number variants (CNVs) noted in relation to the location of known human genes and transcripts from the UCSC Genes track, segmental duplications, microarray (purple), MLPA (light green), and ddPCR (dark green) probe locations, structural variants from the Database of Genomic Variants (DGV), ClinGen, and DECIPHER. Blue bars represent copy number gains (duplications), red bars represent copy number losses (deletions). The minimum and maximum CNV sizes in the clinical CMA cohorts are denoted by thick and thin horizontal bars, respectively.

Article Snippet: CYP2C gene region copy number variants identified by clinical chromosomal microarray (CMA) testing. table ft1 table-wrap mode="anchored" t5 Table 2. caption a7 SAMPLE ID CYP2C19 CYP2C9 Exon 2 Exon 6 Exon 9 Exon 1 Exon 7 Exon 8A Exon 8B Exon 9 ISMMS/Sema4_4 0.499 0.458 0.517 0.928 0.962 0.953 0.989 0.961 ISMMS/Sema4_5 * 0.977 1.030 1.004 1.016 0.995 0.982 0.949 1.075 ISMMS/Sema4_6 0.508 0.903 0.968 0.953 0.959 1.005 1.041 1.014 ISMMS/Sema4_7 0.481 0.854 0.992 1.004 1.010 1.027 1.064 0.984 ISMMS/Sema4_9 1.440 1.665 1.297 1.209 1.561 1.368 1.487 1.577 Open in a separate window * A 113.9 kb deletion was detected by CMA in this sample that included exons 1–8 of CYP2C18 and only exon 1 of CYP2C19 .

Techniques: Microarray

CYP2C gene region copy number variants identified by clinical chromosomal microarray (CMA) testing.

Journal: Human mutation

Article Title: Structural variation at the CYP2C locus: Characterization of deletion and duplication alleles

doi: 10.1002/humu.23855

Figure Lengend Snippet: CYP2C gene region copy number variants identified by clinical chromosomal microarray (CMA) testing.

Article Snippet: CYP2C gene region copy number variants identified by clinical chromosomal microarray (CMA) testing. table ft1 table-wrap mode="anchored" t5 Table 2. caption a7 SAMPLE ID CYP2C19 CYP2C9 Exon 2 Exon 6 Exon 9 Exon 1 Exon 7 Exon 8A Exon 8B Exon 9 ISMMS/Sema4_4 0.499 0.458 0.517 0.928 0.962 0.953 0.989 0.961 ISMMS/Sema4_5 * 0.977 1.030 1.004 1.016 0.995 0.982 0.949 1.075 ISMMS/Sema4_6 0.508 0.903 0.968 0.953 0.959 1.005 1.041 1.014 ISMMS/Sema4_7 0.481 0.854 0.992 1.004 1.010 1.027 1.064 0.984 ISMMS/Sema4_9 1.440 1.665 1.297 1.209 1.561 1.368 1.487 1.577 Open in a separate window * A 113.9 kb deletion was detected by CMA in this sample that included exons 1–8 of CYP2C18 and only exon 1 of CYP2C19 .

Techniques: Microarray, Variant Assay

Journal: Human mutation

Article Title: Structural variation at the CYP2C locus: Characterization of deletion and duplication alleles

doi: 10.1002/humu.23855

Figure Lengend Snippet:

Article Snippet: CYP2C gene region copy number variants identified by clinical chromosomal microarray (CMA) testing. table ft1 table-wrap mode="anchored" t5 Table 2. caption a7 SAMPLE ID CYP2C19 CYP2C9 Exon 2 Exon 6 Exon 9 Exon 1 Exon 7 Exon 8A Exon 8B Exon 9 ISMMS/Sema4_4 0.499 0.458 0.517 0.928 0.962 0.953 0.989 0.961 ISMMS/Sema4_5 * 0.977 1.030 1.004 1.016 0.995 0.982 0.949 1.075 ISMMS/Sema4_6 0.508 0.903 0.968 0.953 0.959 1.005 1.041 1.014 ISMMS/Sema4_7 0.481 0.854 0.992 1.004 1.010 1.027 1.064 0.984 ISMMS/Sema4_9 1.440 1.665 1.297 1.209 1.561 1.368 1.487 1.577 Open in a separate window * A 113.9 kb deletion was detected by CMA in this sample that included exons 1–8 of CYP2C18 and only exon 1 of CYP2C19 .

Techniques: Variant Assay, Microarray