{"database":"ENA","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Fastqsanger.gz":["ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR141/048/SRR14142448/SRR14142448.fastq.gz"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Genomics"],"center_name":["University of Chinese Academy of Science-Shenzhen Hospital"],"full_dataset_link":["https://www.ebi.ac.uk/ena/browser/view/PRJNA719751"],"long_description":["We describe a 4-month-old child with growth and psychomotor retardation, auricle deformity, microcephaly, polydactyly, a heart abnormality, and feeding difficulty. An approximately 12.00 MB deletion was detected in the 8p11.22-p21.2 region."],"repository":["ENA"],"additional_accession":[]},"is_claimable":false,"name":"","description":"Chromosome sequencing","dates":{"last_updated":"2023-05-17","first_public":"2021-04-07"},"accession":"PRJNA719751","cross_references":{}}