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. Author manuscript; available in PMC: 2017 Jun 1.
Published in final edited form as: Heart Rhythm. 2016 May 5;13(8):1652–1660. doi: 10.1016/j.hrthm.2016.05.004

Figure 2.

Figure 2

A: Genetic analysis of proband and family with pipeline for the stratification of rare variants. B: Sanger sequencing in decedent (B-I) and unaffected family member (B-II). C: Genome-wide linkage analysis showing single peak for disease linkage at chromosome 1 at the site of CASQ2. CASQ2 = cardiac calsequestrin 2 gene; CCM2L = cerebral cavernous malformation 2-like gene; CPVT = catecholaminergic polymorphic ventricular tachycardia; EFCAB = EF-hand calcium binding domain gene; InDel = insertion and/or deletion; LOD = logarithm of odds ratio; RYR2 = ryanodine receptor gene; SNV = single nucleotide variant.