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. 2021 Sep 12;16(1):104–115. doi: 10.1002/1878-0261.13091

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© 2021 The Authors. Molecular Oncology published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies

This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

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Fig. 3 — Frequencies of copy number variation and single nucleotide variation in the Side Out 2 trial based on patients’ GMIs. Heat map capturing NGS‐based single nucleotide variations for 22 of the 25 patients enrolled in the Side Out 2 trial; color‐codes reflect the type of alteration harbored by each patient. Legend delfs: deletion‐‐>frameshift; delss: deletion at splice site; expel: deletion at splice site that is expressed in RNA; fs: pm‐‐> frameshift; insfs: insertion‐‐>frameshift; pm: point mutation; pm2: 2‐point mutations; stop: premature stop; ss: splice site; unexpm: unexpressed pm.