fig2

Pregnancy outcomes and short-term follow-up of fetuses with recurrent microdeletion-microduplication syndromes featuring variable penetrance in prenatal diagnosis

Figure 2. Summary and characterization of CNVs in prenatal samples. Resolution based on traditional G-banded karyotyping (> 10 Mb). Positive: CNV detected; Negative: no CNV detected; VOUS: variant of uncertain significance; P: pathogenic; LP: likely pathogenic; CNVs: copy number abnormalities.

Journal of Translational Genetics and Genomics
ISSN 2578-5281 (Online)
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