<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kikas T</submitter><funding>Eesti Teadusagentuur</funding><pagination>574</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9834233</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(1)</volume><pubmed_abstract>Data on the clinical validity of DNA copy number variants (CNVs) in spermatogenic failure (SPGF) is limited. This study analyzed the genome-wide CNV profile in 215 men with idiopathic SPGF and 62 normozoospermic fertile men, recruited at the Andrology Clinic, Tartu University Hospital, Estonia. A two-fold higher representation of > 1 Mb CNVs was observed in men with SPGF (13%, n = 28) compared to controls (6.5%, n = 4). Seven patients with SPGF were identified as carriers of microdeletions (1q21.1; 2.4 Mb) or microduplications (3p26.3, 1.1 Mb; 7p22.3-p22.2, 1.56 Mb; 10q11.22, 1.42 Mb, three cases; Xp22.33; 2.3 Mb) linked to severe congenital conditions. Large autosomal CNV carriers had oligozoospermia, reduced or low-normal bitesticular volume (22-28 ml). The 7p22.3-p22.2 microduplication </pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Microdeletions and microduplications linked to severe congenital disorders in infertile men.</pubmed_title><pmcid>PMC9834233</pmcid><funding_grant_id>PRG1021, IUT34-12</funding_grant_id><pubmed_authors>Reiman M</pubmed_authors><pubmed_authors>Kikas T</pubmed_authors><pubmed_authors>Punab AM</pubmed_authors><pubmed_authors>Punab M</pubmed_authors><pubmed_authors>Tjagur S</pubmed_authors><pubmed_authors>Poolamets O</pubmed_authors><pubmed_authors>Kasak L</pubmed_authors><pubmed_authors>Korrovits P</pubmed_authors><pubmed_authors>Pomm K</pubmed_authors><pubmed_authors>Laan M</pubmed_authors><pubmed_authors>Vihljajev V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Microdeletions and microduplications linked to severe congenital disorders in infertile men.</name><description>Data on the clinical validity of DNA copy number variants (CNVs) in spermatogenic failure (SPGF) is limited. This study analyzed the genome-wide CNV profile in 215 men with idiopathic SPGF and 62 normozoospermic fertile men, recruited at the Andrology Clinic, Tartu University Hospital, Estonia. A two-fold higher representation of > 1 Mb CNVs was observed in men with SPGF (13%, n = 28) compared to controls (6.5%, n = 4). Seven patients with SPGF were identified as carriers of microdeletions (1q21.1; 2.4 Mb) or microduplications (3p26.3, 1.1 Mb; 7p22.3-p22.2, 1.56 Mb; 10q11.22, 1.42 Mb, three cases; Xp22.33; 2.3 Mb) linked to severe congenital conditions. Large autosomal CNV carriers had oligozoospermia, reduced or low-normal bitesticular volume (22-28 ml). The 7p22.3-p22.2 microduplication </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2026-05-28T06:11:12.108Z</modification><creation>2025-04-05T23:31:47.416Z</creation></dates><accession>S-EPMC9834233</accession><cross_references><pubmed>36631630</pubmed><doi>10.1038/s41598-023-27750-w</doi></cross_references></HashMap>