Furthermore, all targeted genes on the designated NGS panel are analyzed for CNVs concurrently; thus, CNV analysis can be extended to all FH-associated genes (in the case of LipidSeq), namely, APOB, PCSK9, LDLRAP1, APOE, STAP1, LIPA, ABCG5, and ABCG8 at no extra cost. The gene discussed is PCSK9; the disease is familial hyperaldosteronism.