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Chunk #19 — Mechanisms of CNV formation

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Origins and functional impact of copy number variation in the human genome.
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We assessed the statistical significance of differences in the breakpoint signatures of deletions and duplications (Supplementary Methods). We found that duplications are more likely to be formed by NAHR, VNTR and retrotransposition, and are more enriched for breakpoint-associated sequence motifs than deletions (Fig. 3a). These findings indicate that the formation of duplications is more likely to be sequence-dependent than deletions.