GM02662
Amniotic fluid-derived cell line from Amniotic fluid
Description:
MARKER CHROMOSOME
Repository
|
NIGMS Human Genetic Cell Repository
|
Subcollection |
Chromosome Abnormalities |
Biopsy Source
|
Amniotic fluid
|
Cell Type
|
Amniotic fluid-derived cell line
|
Transformant
|
Untransformed
|
Sample Source
|
Amniotic fluid-derived cell line from Amniotic fluid
|
Race
|
Black/African American
|
Relation to Proband
|
proband
|
Confirmation
|
Karyotypic analysis after cell line submission to CCR
|
ISCN
|
47,XX,+idic(15)(p13) .ish idic(15)(D15Z1++, SNRPN++, PML-)
|
Species
|
Homo sapiens
|
Common Name
|
Human
|
Remarks
|
|
Passage Frozen |
6 |
|
IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Chromosome Analysis |
|
Cytogenetics |
Chromosome 15: ISOCHROMOSOME Aneuploid Segment (+)15q11>q13 |
Remarks |
47,XX,+mar; unbalanced; marker is de novo and satellited |
Leana-Cox J, Jenkins L, Palmer CG, Plattner R, Sheppard L, Flejter WL, Zackowski J, Tsien F, Schwartz S, Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications. Am J Hum Genet54:748-56 1994 |
PubMed ID: 8178816 |
Passage Frozen |
6 |
Split Ratio |
1:4 |
Temperature |
37 C |
Percent CO2 |
5% |
Medium |
Amniotic Fluid Culture Medium |
Serum |
none Not inactivated |
Substrate |
None specified |
Subcultivation Method |
trypsin-EDTA |
Supplement |
- |
|
|