StudyType	PubMedID	Author	Title	Journal	PublishDate	Chromosome	Disease	Technology	Species	CaseID	Platform	CNA	Connection	Gene	Affiliation	Abstract	GenomeAssembly	GEO	dbGaP	ENA	IsCancer	FusionGene
Research	25043231	Macera MJ, Sobrino A, Levy B, Jobanputra V, Aggarwal V, Mills A, Esteves C, Hanscom C, Pereira S, Pillalamarri V, Ordulu Z, Morton CC, Talkowski M, Warburton D	Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencing.	Prenat Diagn	2015 Mar	3,5,7,9,18	Congenital abnormality	Next Generation Sequencing	Homo sapiens	DGAP259	Next Generation Sequencing			CNTN6;TBC1D5;CNTNAP2;PTPRD;L3MBTL4;LOC1001304840;WDR7	New York Presbyterian Hospital, Columbia University Medical Center, New York, NY, USA	Detection of de novo complex chromosomal rearrangements (CCRs) in prenatal testing is extremely rare.	GRCh37/hg19				No	NA