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. 2019 Jan 11;39(1):BSR20181305. doi: 10.1042/BSR20181305

Figure 1. Rare CNVs identified by a-CGH in three Turners Syndrome patients.

Figure 1

Figure 1

(A) DNA copy number within 7p22.3 region offset down from normal baseline indicates sequence deletions detected by a-CGH in case 16. (B) DNA copy number within 7p22.2 region offset up from normal baseline indicates the sequence repeats detected by a-CGH in case 17. (C) DNA copy number within Xp22.33 region offset up from normal baseline indicates sequence repeats detected by a-CGH in case 6.