Barely Significant
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HBOS-CNV: A New Approach to Detect Copy Number Variations From Next-Generation Sequencing Data.

Front Genet · 2021 · PMC8215577 · PMID 34163521

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extremely significantno p-value reported
The evaluation of genome bins using such a new statistic can lead to less extremely significant CNVs having a high probability of detection.

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