Additional file 2 of Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses

Additional file 2: Table S1. Clinical characteristics of the fetal cases. Table S2. Fetuses with diagnostic or VUS results obtained additional new phenotypes during prenatal and/or postnatal period. Table S3. Fetuses with positive diagnostic results detected by ES. Table S4. Diagnostic rates in different malformation subgroups. Table S5. Diagnostic rates in relation to NT measurement range. Table S6. Number of variants analyzed in step 1 and 2- case by case. Table S7. Number of variants analyzed in step 1 and 2 based on malformation classification or overall result category. Table S8. Fetuses with VUS results detected by ES. Table S9. Fetuses with IFs and SFs results detected by ES. Table S10. Candidate genes identified in this study. Table S11. Pregnancy outcomes of the study cohort.