<p>The first column represents the CNVs detected by CNV-CH in the region 26200000bp–30000000bp of chromosome 20. The second column represents the corresponding percentage of overlap with the regions, reported in the Database of Genomic Variants (DGV), in the same chromosomal section. For a particular row, each entry shows the percentage of overlap of CNV-CH with DGV, EWT, cnMOPS, CNV-TV and CMDs respectively.</p><p>The overlapped percentage of base pairs of CNV regions detected by the aforesaid algorithms.</p
