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. 2022 Nov 5;46(4):829–840. doi: 10.1007/s40618-022-01948-7

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Fig. 3 — Genome-wide DNA study of loss of heterozygosity (LOH) and copy number variation (CNV) in case 3. CNV track shows a gain of chromosome 1 and B-allele frequency (BAF) track shows uniparental disomy of whole chromosome 1