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The 16p11.2 microdeletion probably underlies her abnormal phenotype. The child has carried a de novo 16p11.2 microdeletion, which overlaps with 16p11.2 microdeletion syndrome region, in addition with similar clinical phenotypes. The 16p11.2 microdeletion probably underlies her abnormal phenotype. To carry out genetic diagnosis for a fetus. Chromosome G-banding and chromosomal microarray analysis (CMA) were carried out for a fetus with abnormal morphology of lateral cerebral fissure. The karyotype of the fetus was normal, but CMA showed th
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