Chromosome Analysis Master Panel
A genetic testing panel that evaluates chromosome number and structure for conditions such as developmental delay, birth defects, or infertility.
["This panel can identify certain chromosome abnormalities that may help explain symptoms, guide care, or inform reproductive planning."]
Key facts at a glance
- LOINC
- 62389-2
- Short code
- CHROMOSOMEANALYSISMASTERPANEL
- Synonyms
- —
- Category
- liver
- Sample
- serum
- Container
- Red-top tube (SST)
- Units
- N/A
- Ref low
- 10
- Ref high
- 40
- Critical range
- — – 500 N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- CPT
- 84484
- SNOMED
- 302774002
- Specimen volume
- 5 mL
- Stability
- Room temperature: 4h, Refrigerated: 24h, Frozen: 7d
- Hemolysis max
- 500
- Lipemia max
- 1000
- Icterus max
- 500
- TAT
- 4–24 hours
- Order
- routine
What is this test?
Chromosome analysis examines the chromosomes in a sample of cells to look for differences in chromosome number or structure. A master panel may include several complementary genetic testing methods, so the exact tests included depend on the laboratory and the reason for ordering it.
Why might I need this test?
This testing may be considered for unexplained developmental concerns, multiple birth defects, unusual growth, delayed puberty, infertility, repeated pregnancy loss, or a family history of a chromosome condition. A genetic counselor or clinician can determine whether this panel is appropriate.
How is the test performed?
A laboratory examines chromosomes from patient cells, commonly obtained from a blood sample. The sample is cultured when required, and the chromosomes are analyzed using methods that may include karyotyping, chromosome microarray, or other testing specified by the panel. Special samples, such as amniotic fluid or chorionic villus samples, may be used for prenatal testing.
How do I prepare for the test?
For a routine blood chromosome analysis, fasting is generally not required unless the ordering laboratory gives different instructions. Follow any specimen-specific instructions, particularly for prenatal testing, and tell the care team if you have had a recent bone marrow transplant or received certain cellular therapies.
Reference range
Adult: 10-40 U/LN/A
No special preparation required. Avoid fatty meals before the test if possible.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
An abnormal result may show an extra or missing chromosome, a deleted or duplicated chromosome segment, a balanced rearrangement, or a mixture of cell lines with different chromosome patterns. These findings may help explain a condition or identify reproductive risk, but their meaning depends on the specific result and clinical history. A normal result does not exclude every genetic condition, including some small gene changes or multifactorial disorders, so results should be reviewed with a clinician or genetic counselor.
Short name
Chromosome analysis panel
Frequently asked questions
Does this test diagnose Down syndrome?
Can this test determine whether a chromosome finding came from a parent?
Will the results affect my insurance or employment?
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 17, 2026. · Read our editorial policy