SNP array data for Wilms Tumor harboring de novo germline mutation in CTCF. SNP array data for Wilms Tumor harboring de novo germline mutation in CTCF

SNP array was combined with next generation sequencing (NGS) to identify a unique de novo germline mutation in CTCF that became homozygous in the tumor. SNP array shows an LOH through chr16q where CTCF is located. Overall design: CytoScan HD arrays (Affymetrix) were performed according to the manufacturer's directions on DNA extracted from Wilms tumor sample.