Barely Significant
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Copy number variation associates with mortality in long-lived individuals: a genome-wide assessment.

Aging Cell · 2016 · PMC4717275 · PMID 26446717

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nominally significantno p-value reported
The seven nominally significant CNVs have all, at least partially, been reported by the Database of Genomic Variants (DGV, http://dgv.tcag.ca/dgv/app/home ; Macdonald et al ., 2014 ), supporting that they represent true findings.

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