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Figure 2 | Orphanet Journal of Rare Diseases

Figure 2

From: Comprehensive characterization of malignant phyllodes tumor by whole genomic and proteomic analysis: biological implications for targeted therapy opportunities

Figure 2

Shows genome viewer as reported by Combimatrix positive for high level chromosomal instability (CIN). Amplification of chromosome 1 (CKS1B gene), chromosome 8 (MYC gene), and chromosome 9 (CDKN2A gene) were detected. Deletions of chromosome 17 (TP53 gene), chromosome 10 (GATA3), chromosome 11 (FGF4 and CCND1 genes) and chromosome 22 (PDGFB gene) were also detected.

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172