StudyType	PubMedID	Author	Title	Journal	PublishDate	Chromosome	Disease	Technology	Species	CaseID	Platform	CNA	Connection	Gene	Affiliation	Abstract	GenomeAssembly	GEO	dbGaP	ENA	IsCancer	FusionGene
Research	25736334	Wang JC, Fisker T, Sahoo T	Constitutional chromothripsis involving chromosome 19 in a child with subtle dysmorphic features.	Am J Med Genet A	2015 Apr	19	Dysmorphia	Array CGH	Homo sapiens	25736334_1	4x180 k oligonucleotide array				Cytogenetics Laboratory, Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Ontario, Canada	Chromothripsis is defined as a single event wherein tens to hundreds of chromosomal rearrangements occur in a limited number of genomic regions, although the minimum threshold for the number of breaks and regions involved in chromothripsis has not been defined.	GRCh37/hg19				No	NA