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(A) Frequency of alleles with a single gene copy (n = 195,094) and structural variants (n = 13,924). Structural variants (SV) include copy number variants (CNVs) such as gene deletions and duplications, tandems, and rearrangements. (B) Ethnicity-specific frequency of alleles with a single gene copy and structural variants. Structural variants (SV) include copy number variants (CNVs) such as gene deletions and duplications, tandems, and rearrangements.
