Additional file 6: of Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies
dataset
posted on 2019-06-17, 05:00 authored by Peer Arts, Annet Simons, Mofareh AlZahrani, Elanur Yilmaz, Eman AlIdrissi, Koen Aerde, Njood Alenezi, Hamza AlGhamdi, Hadeel AlJubab, Abdulrahman Al-Hussaini, Fahad AlManjomi, Alaa Alsaad, Badr Alsaleem, Abdulrahman Andijani, Ali Asery, Walid Ballourah, Chantal Bleeker-Rovers, Marcel Deuren, Michiel Flier, Erica Gerkes, Christian Gilissen, Murad Habazi, Jayne Hehir-Kwa, Stefanie Henriet, Esther Hoppenreijs, Sarah Hortillosa, Chantal Kerkhofs, Riikka Keski-Filppula, Stefan Lelieveld, Khurram Lone, Marius MacKenzie, Arjen Mensenkamp, Jukka Moilanen, Marcel Nelen, Jaap Oever, Judith Potjewijd, Pieter Paassen, Janneke Schuurs-Hoeijmakers, Anna Simon, Tomasz Stokowy, Maartje Vorst, Maaike Vreeburg, Anja Wagner, Gijs Well, Dimitra Zafeiropoulou, Evelien Zonneveld-Huijssoon, Joris Veltman, Wendy Zelst-Stams, Eissa Faqeih, Frank Veerdonk, Mihai Netea, Alexander HoischenTable S6. Information on all large >â5-Mb homozygous regions per patient, detected in the exome. Of each region, the genomic location, size, % homozygous variants, and the detected mutation are provided. (XLSX 158 kb)
