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Fig. 1 | BMC Cancer

Fig. 1

From: Combining genomic analyses with tumour-derived slice cultures for the characterization of an EGFR-activating kinase mutation in a case of glioblastoma

Fig. 1

DNA copy number analysis. The genome view generated from aCGH data showed detectable aberrations in the DNA extracted from FFPE primary tumour: gain of chromosomes 2 and 7, loss of the short arm of chromosome 9, and loss of chromosomes 10, 14 and X. The aCGH data also revealed amplification of the q32.1 region (chr 1) and the EGFR gene (chr 7, black arrow), together with a homozygous deletion of the CDKN2A gene (chr 9, black arrow). aCGH: array comparative genomic hybridization; chr: chromosome

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