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Infantile Epilepsy Panel, Sequence Analysis and Exon-Level Deletion/Duplication
2007535
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Ordering Recommendation
Refer to Additional Technical Information document.
Mnemonic
INFAN EPIL
Methodology
Next Generation Sequencing
Performed
Varies
Reported
4-5 weeks
New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
Collect
Lavender (K2 or K3 EDTA). Also acceptable: Pink (K2EDTA).
Specimen Preparation
Transport 5 mL whole blood. (Min: 2 mL)
Test is not performed at ARUP; separate specimens must be submitted when multiple tests are ordered.
Storage/Transport Temperature
Room temperature. Also acceptable: Refrigerated. Protect from extreme temperatures.
Unacceptable Conditions
Remarks
Clinical indication or reason for testing is required.
Stability
Ambient: 1 week; Refrigerated: 1 week; Frozen: Unacceptable
Reference Interval
By report
Interpretive Data
No compliance statements are in use for this test.
Note
Hotline History
Hotline History
Date of Change
Test Name Change
Methodology
Performance/Reported Schedule
Specimen Requirements
Reference Interval
Interpretive Data
Note
CPT Code
Component Change
Other Interface Change
New Test
Inactive
N/A
CPT Codes
81404; 81405; 81406; 81407; 81185
Components
| Component Test Code* | Component Chart Name | LOINC |
|---|---|---|
| 2007536 | Infantile Epilepsy Panel | 35474-6 |
| 2010873 | Ordering Physician Name | 67102-4 |
| 2010874 | Ordering Physician Phone Number | 67714-6 |
| 2010887 | EER Infantile Epilepsy Panel | 11526-1 |
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
Aliases
Infantile Epilepsy Panel, Sequence Analysis and Exon-Level Deletion/Duplication
GeneDx
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