Copy Variants¶
Copy variants should be passed to the IPR python adapter in the main report content JSON.
{
"copyVariants": [
// variants
]
}
Each variant is an object which may contain any of the following fields
Field | Type | Example | Description |
---|---|---|---|
gene (required) | string |
"KRAS" |
the gene name |
kbCategory (required) | string? |
the graphkb copy variant vocabulary term this variant belongs to. By default only amplifications and deep deletions are matched | |
chromosomeBand | string |
"X:p12.2" |
|
cna | number? |
1.22 |
The copy number alteration (CNA) ratio |
copyChange | integer? |
-2 |
the ploidy corrected copy change value |
end | integer? |
the genomic end position of the copy segment this gene copy number was called from | |
log2Cna | number? |
||
lohState | string |
"HET" |
the loss-of-heterozygosity category for this gene region |
start | integer? |
the genomic start position of the copy segment this gene copy number was called from |