Rare copy-number variants as modulators of common disease susceptibility.
Auwerx C, Jõeloo M, Sadler MC et al.
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Abstract
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Copy-number variations (CNVs) have been associated with rare and debilitating genomic disorders (GDs) but their impact on health later in life in the general population remains poorly described.
422 British ancestry cases, 268,280 British ancestry controls
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