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Accession: PRJNA902508 ID: 902508

Whole exome sequencing of Coffin-Siris syndrome patient

In this study, two additional individuals were diagnosed with CSS caused by BAF mutations by whole exon sequencing.
AccessionPRJNA902508
Data TypeRaw sequence reads
ScopeMultispecies
SubmissionRegistration date: 17-Nov-2022
Genetic and Metabolic Central Laboratory, Guangxi Maternal and Child Health Hospital
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments2
Other datasets
BioSample2
SRA Data Details
ParameterValue
Data volume, Gbases31
Data volume, Mbytes3827

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