Fig. 5From: SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing dataCNV result for five methods on adRP patient data. a SeqCNV b CoNIFER c CNVnator d CNVer e XHMM. X-axis represents the genomic position for chromosome chr19. PRPF31 gene is located at chr19:54,618,790–54,635,150. Both SeqCNV and CoNIFER identified the PRPF31 copy number deletionBack to article page