Barely Significant
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Genome-wide analysis of copy number variation in type 1 diabetes.

PLoS One · 2010 · PMC2981564 · PMID 21085585

2
hedged sentences
0.0655
closest p · 1.3× alpha
0.0655
boldest claim

The sentences

approached significancep = 0.0655so close (0.05 < p ≤ 0.1)
While frequency of variance did not differ appreciably between the two groups at CNPs 1162 and 1956, the difference of variance at CNP 1303 approached significance (p = 0.0655).

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