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Lab Dept Anatomic Pathology Test Name COL11A1 DELETION/DUPLICATION HDT ARRAY General Information Lab Order Codes 11DD Synonyms Marshall syndrome COL11A1 Stickler syndrome type II STL2 COL11A1 CPT Codes 81479 Molecular Pathology Unlisted Procedure Test Includes Deletion/Duplication HDT Array uses 60mer oligonucleotide sequences designed to selectively complement target areas with an extremely high degree of specificity.
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Col11a1 deletionduplication hdt array is a specific type of genetic test that is used to detect the presence of deletions or duplications in the COL11A1 gene.
Col11a1 deletionduplication hdt array is typically performed by medical professionals or geneticists who suspect a patient may have a genetic variation in the COL11A1 gene.
Filling out a col11a1 deletionduplication hdt array involves collecting a DNA sample from the individual being tested, performing the genetic analysis using the appropriate laboratory techniques, and interpreting the results based on the presence or absence of deletions or duplications in the COL11A1 gene.
The purpose of col11a1 deletionduplication hdt array is to identify any deletions or duplications in the COL11A1 gene, which is associated with certain genetic disorders and conditions.
The col11a1 deletionduplication hdt array report should include the details of the genetic analysis performed, the presence or absence of deletions or duplications in the COL11A1 gene, and any additional relevant information about the patient's genetic profile.
The specific deadline to file col11a1 deletionduplication hdt array in 2023 may vary depending on the jurisdiction and specific requirements. It is advisable to consult with the relevant medical authorities or genetic testing laboratories for the exact deadline.
The penalties for late filing of col11a1 deletionduplication hdt array, if any, would depend on the regulations of the jurisdiction and the specific circumstances. It is recommended to consult with the relevant authorities for information on any potential penalties.
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