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Understanding Genetic Variability: Exploring Copy Number Variants through Non-Invasive Prenatal Testing in European Populations

2023-08-16

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<title>Abstract</title> <p>CNVs are structural alterations in the genome that involve the duplication or deletion of DNA segments, contributing to genetic diversity and playing a crucial role in evolution and development of various diseases and disorders. Massively parallel sequencing (MPS) has revolutionized the field of genetic analysis and contributed significantly to routine clinical diagnosis and screening....

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Literature Corpus work: 550f7fc9-c72a-551c-b84a-83c06b11c727
DOI: 10.21203/rs.3.rs-3144965/v1

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