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Framework that allows defining file formats (layouts) and use them to read and write data files.
Item #
Length
Source of Standard
Year Implemented
Version Implemented
Year Retired
Version Retired
3801
1
NAACCR
2018
18
NAACCR XML: Tumor.chromosome1pLossHeterozygosity
Description
Chromosome 1p: Loss of Heterozygosity (LOH) refers to the loss of genetic material normally found on the short arm of one of the patient's two copies of chromosome 1. Codeletion of Chromosome 1p and 19q is a diagnostic, prognostic and predictive marker for gliomas and is strongly associated with the oligodendroglioma phenotype.
Rationale
Chromosome 1p: Loss of Heterozygosity (LOH) is a Registry Data Collection Variable in AJCC. It was previously collected as Brain, CS SSF #5.
Codes
0
Chromosome 1p deletion/LOH not identified/not present
1
Chromosome 1p deletion/LOH identified/present
6
Benign or borderline tumor
7
Test ordered, results not in chart
8
Not applicable: Information not collected for this case
(If this item is required by your standard setter, use of code 8 will result in an edit error.)
9
Not documented in patient record
Cannot be determined by the pathologist
Chromosome 1p deletion/LOH not assessed or unknown if assessed
Each Site-Specific Data Item (SSDI) applies only to selected primary sites, histologies, and years of diagnosis. Depending on applicability and standard-setter requirements, SSDIs may be left blank.