Cytogenomic Evaluation of Subjects with Syndromic and Nonsyndromic Conotruncal Heart Defects

Figure 2

The array-CGH profiles of a series of variants of uncertain significance in several cases. (a) An approximately 0.88 Mb duplication at chromosome 1p35.1p34.3 (blue box) in case 56. (b) An approximately 1.0 Mb duplication at chromosome 6q25.2 (blue box) in case 137. (c) An approximately 0.37 Mb deletion at chromosome 7q11.21 (blue box) in case 126. (d) An approximately 0.22 Mb deletion at chromosome 7q31.1 (blue box) in case 360. (e, d) An approximately 0.10 Mb deletion at chromosome 7q31.1 (blue box) in case 49.

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