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Figure 3 | Acta Neuropathologica Communications

Figure 3

From: The prognostic role of intragenic copy number breakpoints and identification of novel fusion genes in paediatric high grade glioma

Figure 3

Intragenic deletions in paediatric high grade glioma. (a) Recurrent copy number breakpoint within NF1 on chromosome 17q11.2 in two cases of pHGG. (b) Recurrent copy number breakpoint within PTPRE on chromosome 10q26.2 in two cases of pHGG. Dark pink: confirmed region of loss; Light pink: region within which breakpoint lies, as defined by the resolution of probes on the array.

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