Barely Significant
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Copy number variation of horse Y chromosome genes in normal equine populations and in horses with abnormal sex development and subfertility: relationship of copy number variations with Y haplogroups.

G3 (Bethesda) · 2022 · PMC9713435 · PMID 36227030

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highly significantP < 0.001actually significant
The Kruskal–Wallis test, on the other hand, showed highly significant ( P < 0.001) CN variation of all genes across breeds, with a slightly lower significance ( P = 0.003) for HSFY ( Table 2 ).

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