Presentation of query results in CNV Workshop. Depicted are results for a chromosome 16 query of sequence position range 20,300,000-20,610,000 in an autism cohort. Top panel: graphical display. Layers (top to bottom) represent the sequence position (top), cytogenetic bands, CNVs observed in the autism cohort, CNVs in the CHOP CNV map, CNVs in the Database of Genomic Variants (labels indicate the study), phenotypes of Genetic Association Database studies, and UCSC Known Genes. All glyphs hyperlink to corresponding database records. Bottom panel: tabular display for a subset of CNVs. Sortable column headers are colored red or (for current sort order) green. Each row value colored red denotes a hyperlink to a corresponding external database record. Checkboxes at far left allow a user to save certain CNVs in the MyCNV clipboard.
Gai et al. BMC Bioinformatics 2010 11:74 doi:10.1186/1471-2105-11-74