Fig. 3From: Identification of established arrhythmogenic right ventricular cardiomyopathy mutation in a patient with the contrasting phenotype of hypertrophic cardiomyopathyThe number of reads in WES and confirmation of the genetic variant by Sanger sequencing. a Whole exome sequencing data showing the number of reads covering the c.2146-1G > C variant in the PKP2 gene. b Sanger sequencing showing heterozygous G > C read out, confirming the WES dataBack to article page