Genotype (CNV and SNP) by Illumina 1MDuo and CBS from ENCODE/HudsonAlpha

ABSTRACT: This data was generated by ENCODE. If you have questions about the data, contact the submitting laboratory directly (Florencia Pauli mailto:[e-mail]). If you have questions about the Genome Browser track associated with this data, contact ENCODE (mailto:[e-mail]). This track is produced as part of the ENCODE project. The track displays copy number variation (CNV) as determined by the Illumina Human 1M-Duo Infinium HD BeadChip assay and circular binary segmentation (CBS). The Human 1M-Duo contains more than 1,100,000 tagSNP markers and a set of ~60,000 additional CNV-targeted markers. The median spacing between markers is 1.5 kb and the mean spacing is 2.4 kb. The B-allele frequency and genotyping single nucleotide polymorphism (SNP) data generated by the experiment

ORGANISM(S): Homo sapiens

SUBMITTER: UCSC ENCODE DCC 

PROVIDER: E-GEOD-40698 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress