Additional file 4: of Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis

Details of rare homozygous variants discovered in 74% (39/53) of the ROH cases that has variants relevant or potentially relevant to the phenotype of the patient. (XLSX 32Â kb)

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Bibliographische Detailangaben
Hauptverfasser:	Prasad, Aparna, Sdano, Matthew, Vanzo, Rena, Mowery-Rushton, Patricia, Serrano, Moises, Hensel, Charles, E. Wassman
Format:	Dataset
Sprache:	eng
Schlagworte:	Biological Sciences not elsewhere classified Cell Biology Computational Biology Developmental Biology FOS: Biological sciences FOS: Mathematics Genetics Mathematical Sciences not elsewhere classified Microbiology Molecular Biology Pharmacology
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Beschreibung
Zusammenfassung:	Details of rare homozygous variants discovered in 74% (39/53) of the ROH cases that has variants relevant or potentially relevant to the phenotype of the patient. (XLSX 32Â kb)
DOI:	10.6084/m9.figshare.6003398