The OncoScan CNV Assay is a whole-genome copy number microarray-based assay that enables the detection of relevant copy number variations (CNVs) such as copy number gain and loss, loss of heterozygosity (LOH), copy neutral loss of heterozygosity (cnLOH), ploidy, allele specific changes, break point determination, mosaicism, clonal heterogeneity, and chromothripsis.
Key features of the OncoScan CNV Assay include:
The assay has the same copy number coverage as the OncoScan CNV Plus Assay but does not include somatic mutation coverage. It provides the reagents for sample preparation from formalin-fixed paraffin-embedded (FFPE) tumor samples and microarray hybridization and staining.
Data analysis is free of charge and easy using one of the three available softwares: Chromosome Analysis Suite (ChAS), Somatic Mutation Viewer 1.1, and Nexus Express software.
DOWNLOADABLE BROCHURE:
OncoScan CNV and CNV Plus Assays
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