Variants Table view

The contents of the Samples column vary by variant type:

  • SNVs and INDELs: Genotype

  • CNVs: Cytoband

  • Fusions: Presence or Absence detection call

Note: In the Variants Table view, analysis columns are ordered from left to right starting with the first analysis that you selected. The annotation data from the variants in the first selected analysis is what populates the Location column of the table.

Restrictions on analysis selection

  • Comparison and visualization are not supported for Metagenomics analyses. If one of these is among the analyses selected, then the Visualize option is not available in the Action menu.

  • If a Failed or In-Progress analysis is among the analyses selected, then the Visualize option is not available in the Action menu.

  • If only one set of variants is selected, the Visualization option is not available:

    • Trio and paired analyses each contain more than one set of variants. These analyses support visualization one a single trio or paired analysis.

    • A tumor-normal analysis has only one set of variants and does not support visualization. (A tumor-normal analysis reports only the set of variants for the tumor sample, not the set of variants for the normal sample.)