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. 2014 Mar 21;9(3):e92695. doi: 10.1371/journal.pone.0092695

Figure 2. Array CGH analysis of chromosome 12.

Figure 2

(A), Array CGH analysis of the entire chromosome 12 in the patient, showing a 14-Mb deletion of 12q21.2–q21.33 (77.2–91.2 M). (B), Detailed views of the microarray plots for the patient and his parents. The vertical axis shows megabases (Mb) from the telomere of 12q, and the horizontal axis shows the fold-change in copy number variation. (C), Comparison of the deleted positions. Bars indicate the deletion of the patient. (1) our patient, (2) Rauen, et al., 2002, (3) Klein, et al., (4) Brady, et al., and (5) Rauen, et al., 2000, respectively. The main genes existing in this area were listed as modified NCBI data. Genes surrounding LIN7A, from ZDHHC17 to DUSP6, which are enclosed by the square, were included in the common deleted region from all five cases. An asterisk indicates LIN7A.