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Test Name: | Chromosome 1p/19q Deletion Detection |
Compliance: | CE-IVD |
Test Description: | Combined loss of chromosomal arms 1p and 19q resulting from an unbalanced t(1;19)(q10;p10) translocation leads to the loss of one hybrid chromosome and thus loss of heterozygosity. This cytogenetic aberration is strongly associated with oligodendrogliomas. This test aims to identify co-deletion of the chromosome 1p/19q in oligodendrogliomas patients. |
Methodology: | Fluorescent in Situ Hybridization (FISH) Analysis |
Gene Name: | |
Protein Name: | |
Specimen Requirements: | FFPE Slides: 5-10 4µm FFPE tissue unstained sections on coated slides. One section must be stained with H&E and mounted with tumor region (area of interest) marked. Please include a copy of corresponding surgical pathology report. FFPE Block: Paraffin-embedded, formalin-fixed tissue block containing adequate amounts of tumor to be analyzed with areas of tumor marked. Please include a copy of corresponding surgical pathology report. |
Storage Condition: | Room Temperature |
Turn Around Time: | 3-5 working days from day of specimen received |
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Genetic Home Reference: | |
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We may also disclose medical information about you to authorised public health or government officials for public health activities as required by law.
Copyright © 2013 香港分子病理檢驗中心 Hong Kong Molecular Pathology Diagnostic Centre Limited (HKMPDC). All Rights Reserved.
Information Updated 29 June, 2020.
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