ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR141/048/SRR14142448/SRR14142448.fastq.gzprimaryOK200GenomicsUniversity of Chinese Academy of Science-Shenzhen Hospitalhttps://www.ebi.ac.uk/ena/browser/view/PRJNA719751We 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.ENAfalseChromosome sequencing2023-05-172021-04-07PRJNA719751