Universal chromosomal microarray analysis reveals high proportion of copy-number variants in low-risk pregnancies

Keyphrases

• Copy number Variation 100%
• Low-risk Pregnancy 100%
• Chromosomal Microarray 100%
• Clinically Significant 66%
• Ultrasound 50%
• Genetic Testing 50%
• High-risk Pregnancy 50%
• Early Onset 33%
• Penetrance 33%
• Susceptibility Loci 33%
• Early Disease 33%
• Pathogenic Copy number Variant (pCNV) 33%
• Abnormal Ultrasound 33%
• Medical Records 16%
• Pregnant Women 16%
• Large Cohort 16%
• Pregnancy Outcome 16%
• Background Risk 16%
• Low-risk Group 16%
• Prenatal Genetic Testing 16%
• Ultrasound Abnormalities 16%

Biochemistry, Genetics and Molecular Biology

• Array Comparative Genomic Hybridization 100%
• Genetic Screening 50%
• Prevalence 50%
• Penetrance 33%
• Medical Record 16%
• Pregnancy 16%
• Low Risk Population 16%
• Genetic Prenatal Diagnosis 16%