The role of BCL9 genetic variation as a biomarker for hepatitis C-related hepatocellular carcinoma in Egyptian patients.

Copy number variations have been discovered as intra-species alterations, which occurs as a repeating of a sequence of nucleotides in tandem multiple times in an individual’s genome, including insertion (gain) or deletion (loss) of genetic material with a highly significant biological role; they range in the human genome from 10 kb to 1 Mb in size and cover about 12% of the human genome [ 19 , 20 ].

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