Large scale copy number variation (CNV) at 14q12 is associated with the presence of genomic abnormalities in neoplasia.

BMC Genomics · 2006 · PMC1550726 · PMID 16756668

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a slight trendp ≤ 1not close (p > 0.1)

Comparison of the number of variants in CNV14q12 seen in CML patients with and without a der(9) deletion showed a slight trend but no statistical difference in the frequency of the CNV14q12 variation in the presence of a der(9) deletion (p ≤ 1).

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