CNV

The 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.

The following workflows and/or categories are available:

• CEL-CNV-EACON (⤫ LEGACY)
• EACON-CYTOSCAN (✓ PRODUCTION)
• EACON-ONCOSCAN (✓ PRODUCTION)