Cell-free DNA (cfDNA) quantitative analysis using a specific genetic probe (e.g., for tumor DNA detection)
This test measures tiny pieces of DNA found naturally in your bloodstream, often used to detect genetic material from tumors or other conditions.
["This test helps identify abnormal DNA that may signal cancer or other genetic changes."]
Key facts at a glance
- LOINC
- 4999-9
- Short code
- CMV DNA Ur Ql NAA+probe
- Synonyms
- CMV DNA Ur Ql NAA+probe
- Category
- chemistry
- Sample
- urine
- Container
- Sterile urine container
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- probe-amp-tar
- Specimen volume
- 10 mL
- Stability
- Room temperature: 2h, Refrigerated: 24h, Frozen: 7d
- Hemolysis max
- 0
- Lipemia max
- 0
- Icterus max
- 0
- TAT
- 4–24 hours
- Order
- routine
What Is This Test Measuring?
Your blood contains small fragments of DNA called cell-free DNA (cfDNA). This test focuses on detecting specific sequences of DNA, often linked to cancer or other genetic conditions, using a specialized genetic probe. The probe binds to particular DNA sequences that may be present in higher amounts in certain diseases.
Why Might You Need This Test?
This test may be used in certain situations, such as monitoring for cancer recurrence, guiding treatment decisions, or assessing genetic risks in specific clinical scenarios. It is particularly relevant in oncology for detecting tumor DNA that may not be visible on standard imaging.
How Is the Sample Collected?
A blood sample is drawn from a vein, typically in your arm. The blood is processed to separate the cell-free DNA from the rest of the blood components. The genetic probe is then used to analyze the DNA fragments for specific sequences.
What Does the Result Mean?
Results are qualitative (present or absent) or quantitative (relative concentration) for the specific DNA sequences tested. A positive result may indicate the presence of abnormal DNA, such as from a tumor, but further evaluation by a healthcare provider is needed to interpret the clinical significance.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
◆Associated findings1
Frequently asked questions
What does a positive result mean?
How often is this test repeated?
Can this test detect all types of cancer?
Sources
- 1
- 2Lab Tests OnlineSource
- 3
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy