Barely Significant
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Using the linear references from the pangenome to discover missing autism variants.

Nat Commun · 2026 · PMC12909954 · PMID 41577710

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a suggestive trendno p-value reported
We find no evidence of increased autosomal SV burden for probands when compared to unaffected siblings yet observe a suggestive trend toward an increased SV burden on the X chromosome among affected females.

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