The 12-sample HumanCytoSNP-12 BeadChip is a powerful whole-genome scanning panel designed for efficient, high-throughput analysis of genetic and structural variations that are relevant to human diseases. This scalable, proven solution offers substantially better resolution to detect smaller regions than fluorescence in situ hybridization (FISH) or comparative genomic hybridization (CGH).1
The HumanCytoSNP-12 BeadChip is optimized to detect cytogenetic abnormalities most relevant to human disease.1-2 Content includes ~300,000 SNPs targeting regions shown to be important for cytogenetic analysis. The result is dense coverage of ~250 disease regions, including subtelomeric regions, pericentromeric regions, and sex chromosomes, commonly screened in cytogenetics labs. Sufficient SNP coverage is provided to determine dosage sensitivity of > 800 genes.
View manifest (array content) filesCustom Cluster File Creation for Improved Copy Number Analysis
Technical Note | PDF < 1 MB
Cytogenetics to Cytogenomics: An Introduction to Genomic Technologies
White Paper | PDF 2 MB
Infinium HumanCytoSNP-12 v2.1 BeadChip
Data Sheet | PDF < 1 MB