Fig. 3
From: cnvCurator: an interactive visualization and editing tool for somatic copy number variations
The breakpoint alignment of the missed CNV call. The shown region in the main window is base pairs 116025000-121875000 on chromosome 4. The two vertical lines (red on the left, and green on the right) in the main window delimit the boundary of the segment of copy number loss (Chr4: 117112372-120460622) missed by CONSERTING as described in Fig. 2, with the breakpoint alignments displayed in the two separate pop-up windows