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. 2019 Dec 9;2(1):vdz051. doi: 10.1093/noajnl/vdz051

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© The Author(s) 2019. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 1. — Genomic landscape of samples included in the INTELLANCE-2/EORTC_1410 trial. Shown are waterfall plots of chromosomal changes (A), gains and losses of individual genes (B), and SNVs within individual genes (C). The copy number changes, gene amplifications/deletions, and mutations are similar to observed in other (EGFR-amplified) glioblastoma datasets. Patients included in this study therefore were not selected for a specific molecularly subtype. LOH = loss of heterozygosity; HD = homozygous deletion.