11
edits
Changes
STBT5:Solitary fibrous tumour (view source)
Revision as of 17:07, 27 February 2024
, 17:07, 27 February 2024→Individual Region Genomic Gain / Loss / LOH
Line 87:
Line 87:
7+chr7:1-159,335,973 [hg38]+chr7+Presence of monosomy 7 (or 7q deletion) is sufficient for a diagnosis of AML with MDS-related changes when there is ≥20% blasts and no prior therapy (add reference). Monosomy 7/7q deletion is associated with a poor prognosis in AML (add reference).
8+chr8:1-145,138,636 [hg38]+chr8+Common recurrent secondary finding for t(8;21) (add reference).
Co-deletion of 1p and 18q+See chromosomal rearrangements table as this pattern is due to an unbalanced derivative translocation associated with oligodendroglioma (add reference).
!Notes
!Notes
|-
|-
−|<span class="blue-text">EXAMPLE:</span>
+|
−|
−|<span class="blue-text">EXAMPLE:</span> Loss
+|
−|<span class="blue-text">EXAMPLE:</span>
+|
−|
−|<span class="blue-text">EXAMPLE:</span>
+|
−|
−|<span class="blue-text">EXAMPLE:</span> Yes
+|
−|<span class="blue-text">EXAMPLE:</span> Yes
−|<span class="blue-text">EXAMPLE:</span> No
−|<span class="blue-text">EXAMPLE:</span>
−|-
|-
−|<span class="blue-text">EXAMPLE:</span>
+|
−|
−|<span class="blue-text">EXAMPLE:</span> Gain
+|
−|<span class="blue-text">EXAMPLE:</span>
+|
−|
−|<span class="blue-text">EXAMPLE:</span>
+|
−|
−|<span class="blue-text">EXAMPLE:</span> No
+|
−|<span class="blue-text">EXAMPLE:</span> No
−|<span class="blue-text">EXAMPLE:</span> No
−|<span class="blue-text">EXAMPLE:</span>
−|}
|}
==Characteristic Chromosomal Patterns==
==Characteristic Chromosomal Patterns==
−Not Applicable
Not Applicable
Line 125:
Line 116:
!Notes
!Notes
|-
|-
−|<span class="blue-text">EXAMPLE:</span>
+|
−|
−|<span class="blue-text">EXAMPLE:</span> Yes
+|
−|<span class="blue-text">EXAMPLE:</span> No
+|
−|<span class="blue-text">EXAMPLE:</span> No
+|
−|<span class="blue-text">EXAMPLE:</span>
−|}
|}
==Gene Mutations (SNV / INDEL)==
==Gene Mutations (SNV / INDEL)==