Microarray Chromosome Testing (Chromosome Structure Mutation Analysis)

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chromosomal test
chromosomal tests for congenital anomalies
Microarray Chromosome Testing (Chromosome Structure Mutation Analysis)

Laboratory：Akiruno

○Microarray Chromosome Testing (Chromosome Structure Mutation Analysis)

CODE：00E37 6

TEST NAME SPECIMEN
REQUIREMENT
（ｍL） CONTAINER CAP COLOR STORE
TEMPERATURE
(STABILITY) TURNAROUND
TIME (DAY) METHODOLOGY REFERENCE RANGE
(UNIT)
Microarray Chromosome Testing (Chromosome Structure Mutation Analysis)
Blood (EDTA-2Na added)
7.0
PN7
（7 days）
7-16 Array CGH method
Array CGH method
The principle of comparative genomic hybridization (CGH), which detects copy number changes (CNV) such as amplifications and deletions that occur in the genome by comparing fluorescently labeled sample-derived DNA and normal cell-derived DNA. This method is a combination of microarray technology.

COMMENT

Avoid freezing. Please indicate sex, clinical diagnosis and clinical findings on the request form. Please consult us if the required sample volume is not met in neonatal blood collection.
Submit the specimen on the same day after collection. Collect blood in the designated container, mix well, and preserve refrigerated.
About Submission of Chromosome Testing Submit the specimen on the same day after collection.
Subject to ethical guidelines (see below)
Collect blood in the designated container, mix well, and preserve refrigerated. Please submit the specimen on the same day after blood collection. Avoid duplicate requests of other items.