Skip to main content
Figure 4 | BMC Bioinformatics

Figure 4

From: "GenotypeColour™": colour visualisation of SNPs and CNVs

Figure 4

Genomic CNV table. List of all CNVs identified in four samples. All the compared samples are reported in the same table. Each sample is represented by four columns (from column 2 to the second-last): first column, the number of SNPs involved in the CNV; second column, the start position (in bp) of the CNV; third column, the end position of the CNV; fourth column, the type of CNV (deletion or duplication). The CNVs, identified in different samples that share at least a partially overlapping fragment, are reported in the same row. So, each row represents a different CNV and the number of rows corresponds to the number of different CNVs identified in all compared samples. The first column of the table reports the chromosome where the CNVs are located, the last column reports the name of the equivalent variations in the Database of Genomic Variants (DGV) [7], when present. The three CNVs on chromosome 15 of the first four samples of Figure 3 are highlighted by a red square.

Back to article page