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 the most relevant to human disease. It offers substantially better resolution to detect smaller regions than FISH or CGH. Studies can achieve average SNP call rates and reproducibility of >99%, and low noise for copy number measurements.Many types and sizes of structural variation in the human genome that affect phenotypes can be detected with the HumanCytoSNP-12 BeadChip, including duplications, deletions, amplifications, copy-neutral LOH, and mosaicism.
This BeadChip includes a complete panel of genome-wide tag SNPs and markers targeting all regions of known cytogenetic importance. It incorporates 200,000 “best of the best” SNPs with the highest tagging power.
220,000 markers provide useful content for cytogenetic analysis. This includes dense coverage of around 250 genomic regions commonly screened in cytogenetics laboratories, including subtelomeric regions, pericentromeric regions, sex chromosomes, and targeted coverage in around 400 additional disease-related genes.
Downstream data analysis is fully supported with Illumina's GenomeStudio software.
Catalog IDs: WG-320-2101, WG-320-2102, WG-320-2103, WG-320-2104, WG-320-2105