<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Vcf>ftp://ftp.sra.ebi.ac.uk/vol1/analysis/ERZ248/ERZ24834603/Sample.vcf.gz</Vcf><Other>ftp://ftp.sra.ebi.ac.uk/vol1/analysis/ERZ248/ERZ24834603/Sample.vcf.csi</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>European Bioinformatics Institute</center_name><center_name>Nanjing Maternity and Child Health Care Hospital, Prenatal Diagnosis</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJEB79890</full_dataset_link><broker_name>EBI</broker_name><scientific_name>Homo sapiens</scientific_name><long_description>Identification of precise breakpoints of structural variations in a Chinese girl with syndromic developmental delay</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name></name><description>Investigation of human structural variations</description><dates><last_updated>2024-09-15</last_updated><first_public>2024-09-12</first_public></dates><accession>PRJEB79890</accession><cross_references><taxon>9606</taxon></cross_references></HashMap>