{"database":"GEO","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Other":["ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE171nnn/GSE171207/"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Genomics"],"species":["Homo sapiens"],"gds_type":["Genome variation profiling by high throughput sequencing"],"full_dataset_link":["https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE171207"],"repository":["GEO"],"entry_type":["GSE"],"additional_accession":[]},"is_claimable":false,"name":"Single-cell CNV dataset by Cell Ranger from severe aplastic anaemia patients","description":"Single Cell CNV experiment was performed in severe aplastic anaemia patients with known chromosome 7 abnormality. The goal of this project is to use single cell CNV to assess whether these abnormalities existed prior to immunosuppressive treatment (baseline) and were just too small to detect it with standard cytogenetics.","dates":{"publication":"2026/05/31"},"accession":"GSE171207","cross_references":{"GSM":["GSM5220833","GSM5220822","GSM5220834","GSM5220823","GSM5220835","GSM5220824","GSM5220836","GSM5220825","GSM5220830","GSM5220831","GSM5220820","GSM5220832","GSM5220821","GSM5220819","GSM5220826","GSM5220837","GSM5220838","GSM5220827","GSM5220816","GSM5220839","GSM5220828","GSM5220817","GSM5220829","GSM5220818"],"GPL":["24676"],"SRA":["SRP312799"],"GSE":["171207"],"taxon":["Homo sapiens"],"PMID":["[42047559]"]}}