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. 2019 Dec 11;11(12):1992. doi: 10.3390/cancers11121992

Figure 3.

Figure 3

(a) Copy number analysis by CCCP. The log2-fold change for each gene is shown. SMARCB1 (indicated by arrow) on chromosome 22 shows a fold change consistent with biallelic deletion. (b) Cancer whole exome sequencing (CWES) was performed in two cases and confirmed bi-allelic SMARCB1 gene deletion involving chromosome 22q11.2.