Barely Significant
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De novo and inherited CNVs in MZ twin pairs selected for discordance and concordance on Attention Problems.

Eur J Hum Genet · 2012 · PMC3449078 · PMID 22490988

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nominally significantno p-value reported
Genome-wide CNV burden and AP There was a nominally significant association with AP and the average size of CNVs within genes, where the affected individuals had larger CNV events than the unaffected group (>120 kb more on average, P =0.00830, cf. a level of 0.00833 (=0.05/6) maintains a family-wise type-I error of 0.05, Table 2 ).

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