Brain Tumor : 1p/19q Co-Deletion Analysis

Test Information

Turnaround Time

10 days

CPT Code(s)





1p/19q Co


Clinical Information

Loss of heterozygosity (LOH) at 1p19q due to derivative chromosome loss from an unbalanced translocation t(1:19)(q10:p10) is reported to occur with a frequency of ~40% in patients with oligoastrocytoma and 60-80% in oligodendrogliomas. Interestingly, 1p/19q co-deletion is only found in patients with a concomitant alteration in IDH1. Additionally, these patients have been shown to have better prognosis than those having only IDH1 mutated. While this supports the prognostic value of 1p/19q co-deletion, this alteration has also been found to have predictive value in gliomas. Carriers have increased survival compared to non-carriers as well as increased sensitivity to a specific chemotherapeutic regimen (procarbazine, lomustine, and vincristine) (Annals of Translational Medicine (2015) 3(7): 95).


Gene sequencing and targeted mutation testing and copy number analysis can serve as a useful diagnostic and potentially prognostic tool for the analysis of affected tissues or tumors. The detection of copy number variants or specific gene mutations may enhance treatment decisions.

Specimen Requirements

Analysis can be performed on fresh or frozen tissue samples as well as formalin-fixed, paraffin-embedded tissue samples.

Transport Instructions

The specimen should be kept at the appropriate temperature and delivered via overnight shipping.

Have Questions Need Support?

Call our laboratory at 1-800-473-9411 or contact one of our Laboratory Genetic Counselors for assistance.
Robin Fletcher, MS, CGC
Kellie Walden, MS, CGC

Oncology Testing, Targeted Variants
Meet Reggie Roper

Meet Reggie Roper

Reggie has been part of the GGC family for over 18 years. He has short stature, webbing of his hands, pulmonary stenosis, seizures and hydrocephalus along with developmental delay. He carried an initial diagnosis of cardiofaciocutaneous (CFC) syndrome; however, as genetic testing advanced, GGC made the diagnosis of Noonan-like syndrome with loose anagen hair by identifying a mutation in the SHOC2 gene. He is also an active participant in the Greenwood Community Theatre's Penguin Project. "GGC is...

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