CLL NGS PANEL FISH and KT and IGVH Mutation Analysis and NGS TP53 Mutation Analysis Test
Test Name: CLL NGS PANEL FISH and KT and IGVH Mutation Analysis and NGS TP53 Mutation Analysis
Components: Sodium Heparin Vacutainer (2ml) + EDTA Vacutainer (2ml)
Price: 9360.0 AED
Sample Condition: Peripheral blood + FFPE BLOCK
Report Delivery: 15-18 days
Method: Cell Culture + FISH + PCR + NGS
Test Type: Genetics
Doctor: Gynecologist
Test Department: Pre Test Information
CLL NGS PANEL (FISH + KT + IGVH Mutation Analysis + NGS TP53 Mutation Analysis) can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.
Test Details:
The CLL NGS panel is a comprehensive genetic testing panel that combines several different tests to provide a comprehensive analysis of chronic lymphocytic leukemia (CLL). The panel includes fluorescence in situ hybridization (FISH), karyotyping (KT), IGVH mutation analysis, and NGS TP53 mutation analysis.
FISH is a technique used to detect specific genetic abnormalities in CLL cells. This test is useful for identifying common chromosomal abnormalities associated with CLL, such as deletion of chromosome 13q, deletion of chromosome 11q, and trisomy 12.
KT is a test that examines the structure and number of chromosomes in CLL cells. This test can identify large-scale chromosomal abnormalities, such as translocations or deletions, that may be missed by FISH.
IGVH mutation analysis is a test that examines the mutations in the immunoglobulin variable region genes. This test is important for predicting the course of the disease and response to treatment.
NGS TP53 mutation analysis is a test that examines mutations in the TP53 gene, which is commonly mutated in CLL. This test is important for predicting treatment response and overall prognosis.
By combining these tests, the CLL NGS panel provides a comprehensive analysis of CLL genetics, which can help guide treatment decisions and improve patient outcomes.
Test Name | CLL NGS PANEL FISH andKT and IGVH Mutattion Analysisand NGS TP53 mutation analysis Test |
---|---|
Components | Sodium Heparin Vacutainer (2ml)+ EDTA Vacutainer (2ml) |
Price | 9360.0 AED |
Sample Condition | Peripheral blood + FFPE BLOCK |
Report Delivery | 15-18 days |
Method | Cell Culture + FISH+PCR+NGS |
Test type | Genetics |
Doctor | Gynecologist |
Test Department: | |
Pre Test Information | CLL NGS PANEL (FISH +KT + IGVH Mutattion Analysis+ NGS TP53 mutation analysis) can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad. |
Test Details |
The CLL NGS panel is a comprehensive genetic testing panel that combines several different tests to provide a comprehensive analysis of chronic lymphocytic leukemia (CLL). The panel includes fluorescence in situ hybridization (FISH), karyotyping (KT), IGVH mutation analysis, and NGS TP53 mutation analysis. FISH is a technique used to detect specific genetic abnormalities in CLL cells. This test is useful for identifying common chromosomal abnormalities associated with CLL, such as deletion of chromosome 13q, deletion of chromosome 11q, and trisomy 12. KT is a test that examines the structure and number of chromosomes in CLL cells. This test can identify large-scale chromosomal abnormalities, such as translocations or deletions, that may be missed by FISH. IGVH mutation analysis is a test that examines the mutations in the immunoglobulin variable region genes. This test is important for predicting the course of the disease and response to treatment. NGS TP53 mutation analysis is a test that examines mutations in the TP53 gene, which is commonly mutated in CLL. This test is important for predicting treatment response and overall prognosis. By combining these tests, the CLL NGS panel provides a comprehensive analysis of CLL genetics, which can help guide treatment decisions and improve patient outcomes. |