Fig. 1
From: The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young
CONSORT diagram of decedents selected for genome sequencing. Phenotype data were made available by the SDY Case Registry after cause of death was determined. * Indicates the following: DUA constraints limited the sharing of detailed phenotypic data from some cases; all cases were reviewed locally and centrally by the SDY Case Registry and met inclusion criteria. These cases were considered as “Phenotype not available to include”. GS, genome sequencing