Figure 2 | Scientific Reports

Figure 2

From: Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center retrospective study

Figure 2

Other detected pathogenic copy number variants associated with CNS anomalies. (A) A 28.6 Mb deletion in the 13q31.1q34 region was detected in Case 1 by chromosomal microarray analysis. (B,C) In Case 2, a 7q32.1q36.3 duplication combined with a 10q26.2q26.3 microdeletion was identified using chromosomal microarray analysis. (D) In Case 5, a 4p16.3p16.2 microdeletion and a 4p16.2p15.1 duplication were detected using chromosomal microarray analysis. (E) A 20.2 Mb duplication in the 2p25.3p24.1 region was observed in Case 9 using chromosomal microarray analysis.

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