Fig. 2 | Nature Communications

Fig. 2

From: Genomic analysis identifies frequent deletions of Dystrophin in olfactory neuroblastoma

Fig. 2

Detection of a 27 kb deletion in DMD. High density SNP array (850k chip) detected a 27 kb deletion of the DMD gene in an ONB from a male patient (ENBBG-T, Table 1). The panel on the left (a) shows the array profile of the entire chromosome X, with indicated deletion in Xp21.1. The panel on the right (b) focuses on the region of Xp21.1 containing the DMD gene. The deletion is within the DMD gene, from genomic position 32,814,846–32,842,232 (hg19)

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