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Analysis of copy number variants detected by sequencing in spontaneous abortion

Analysis of copy number variants detected by sequencing in spontaneous abortion

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_eb43b69c8ea349bca659aea0c48fefb1

Analysis of copy number variants detected by sequencing in spontaneous abortion

About this item

Full title

Analysis of copy number variants detected by sequencing in spontaneous abortion

Publisher

England: BioMed Central Ltd

Journal title

Molecular cytogenetics, 2024-05, Vol.17 (1), p.13-13, Article 13

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

The incidence of spontaneous abortion (SA), which affects approximately 15-20% of pregnancies, is the most common complication of early pregnancy. Pathogenic copy number variations (CNVs) are recognized as potential genetic causes of SA. However, CNVs of variants of uncertain significance (VOUS) have been identified in products of conceptions (POCs...

Alternative Titles

Full title

Analysis of copy number variants detected by sequencing in spontaneous abortion

Authors, Artists and Contributors

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Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_eb43b69c8ea349bca659aea0c48fefb1

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_eb43b69c8ea349bca659aea0c48fefb1

Other Identifiers

ISSN

1755-8166

E-ISSN

1755-8166

DOI

10.1186/s13039-024-00683-3

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