Barely Significant
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Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.

Lancet · 2010 · PMC2965350 · PMID 20888040

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highly significantno p-value reported
We identified a highly significant excess of large, rare CNVs in children with ADHD compared with control participants, with the average number of CNVs per child with ADHD being 2·09 times higher than that in controls (p=8·9×10 −5 table 1 ). 50 (14%) affected children were shown to carry a CNV larger than 500 kb, compared with 75 (7%) controls.

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