Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants

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Acknowledgments

For technical support and expertise we thank the High Throughput Sequencing and Microarray Units of the DKFZ Genomics and Proteomics Core Facility. This work was principally supported by the PedBrain Tumor Project contributing to the International Cancer Genome Consortium, funded by German Cancer Aid (DKH, #109252) and by the German Federal Ministry of Education and Research (BMBF, #01KU1201A, MedSys #0315416C and NGFNplus #01GS0883). Additional support came from the German Cancer Research Center—Heidelberg Center for Personalized Oncology (DKFZ-HIPO).

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Correspondence to David T. W. Jones or Victor F. Mautner.

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Hutter, S., Piro, R.M., Reuss, D.E. et al. Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants. Acta Neuropathol 128, 449–452 (2014). https://doi.org/10.1007/s00401-014-1311-1

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Keywords

  • COQ6
  • Copy Number Alteration
  • Whole Exome Sequencing
  • Somatic Mosaicism
  • Copy Number Profile