Fig. 2From: CNV Radar: an improved method for somatic copy number alteration characterization in oncologySchematic diagram for assigning copy number types to each genomic segment that was defined by identified breakpoints. mCNV, median copy number variation; CNV, copy number variation; mLFC, median log2 fold change; LFC, log2 fold change; mVAF, median variant allele frequency; VAF, variant allele frequency; LOH, loss of heterozygosityBack to article page