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Mutations and CNV information of 74 NRmRNAs in CESC. (A) Ninety-seven out of 289 patients show different genetic alterations, including nonsense mutations, splice-site mutations and missense mutations. (B) CNV of 74 NRmRNAs: Columns: CNV frequency; Red dots: CNV amplification; Green dots: deletion of CNV. (C) Location of CNV alterations in the intracellular NRmRNAs: Red: high frequency of increased NRmRNAs copy number; Blue: high frequency of deleted NRmRNAs copy number.
