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. 2019 Sep 13;9:871. doi: 10.3389/fonc.2019.00871

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Copyright © 2019 Thakral, Kaur, Gupta, Benard-Slagter, Savola, Kumar, Anand, Rani, Verma, Joshi, Kumar, Sharma, Bakhshi, Seth and Singh.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Frequency distribution of CNAs in ALL cases analyzed by dMLPA. (A) Gene deletions detected in samples of B-ALL (filled red bar) and T-ALL (Empty red bar) are shown in the left panel and gene duplications (filled and empty green bars, respectively) in the right panel. (B) Bar diagram showing percentage of cases with 0, 1, 2, and ≥3 CNAs, GA represents recurrent genetic chromosomal abnormalities.