GEOapplication/xmlftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE335nnn/GSE335495/primaryOK200GenomicsHomo sapiensGenome variation profiling by genome tiling arrayhttps://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE335495GEOGSEfalseContribution of chromosomal aneuploidy and submicroscopic copy number variations (CNVs) in recurrent pregnancy loss (RPL)This study investigates the contribution of chromosomal aneuploidy and submicroscopic copy number variations (CNVs) in recurrent pregnancy loss (RPL). Genomic DNA from RPOC samples was analyzed using high-resolution Agilent aCGH arrays (180K). Several clinically relevant CNVs, including deletions and amplifications affecting immune-related and developmental genes, were identified. This suggests a genetic predisposition underlying some cases of RPL.2026/06/19GSE335495GSM9814650GSM9814651GSM9814647GSM9814648GSM9814656GSM9814645GSM9814646GSM9814657GSM9814654GSM9814655GSM9814652GSM9814653GSM981464937117335495Homo sapiens