Fig. 4From: SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing dataaCGH validation of copy number deletion in PRPF31 gene for sample UTAD082. The shaded area indicates the CNV area with loss of one copy of the genomic segment. Validation results for other 4 samples can be found in Additional file 1 . Five samples share different deletion sizes, ranging from several exons to entire genomic region of PRPF31 Back to article page